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Interfacial degradation of the NMC/LiPSCl composite cathode in all-solid-state batteries
Ist Teil von
Journal of materials chemistry. A, Materials for energy and sustainability, 2024-02, Vol.12 (6), p.37-371
Erscheinungsjahr
2024
Quelle
Alma/SFX Local Collection
Beschreibungen/Notizen
Mitigating interfacial reactions in composite cathode materials remains a key challenge for high-performance all-solid-state batteries (ASSBs), particularly those employing argyrodite-based electrolytes coupled with high-voltage cathodes. Here we study the interfacial chemical reactivity of a Li
1−
x
Ni
0.5
Mn
0.3
Co
0.2
O
2
(NMC532) and Li
6
PS
5
Cl (LPSC) composite using galvanostatic electrochemical impedance spectroscopy, complemented by surface and bulk-sensitive X-ray techniques. By decoupling the time-dependent interfacial degradation from the overall degradation, we show that the redox reaction between NMC532 (oxidant) and LPSC (reductant) is the main origin of degradation. The chemical reaction products share chemical similarities with the ones after the electrochemical reaction. The analysis shows the oxidation activity of transition metals in the cathode composite is Ni
4+/3+
> Mn
4+
/Co
3+
> Ni
2+/3+
. Molecular-dynamics simulations reveal that the reaction is driven by the Li
+
diffusion from LPSC to the delithiated-NMC532, leading to the LPSC's structural decomposition and collapse.
Mitigating interfacial reactions in composite cathode materials remains a key challenge for high-performance all-solid-state batteries (ASSBs), particularly those employing argyrodite-based electrolytes coupled with high-voltage cathodes.
Sprache
–
Identifikatoren
ISSN: 2050-7488
eISSN: 2050-7496
DOI: 10.1039/d3ta06092f
Titel-ID: cdi_rsc_primary_d3ta06092f
Format
–
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